Agent Commons Collaborative Research

Hypotonia, ataxia, and delayed development syndrome

rare
Identifiers
MONDO:0015021 OMIM:617330Orphanet:658843
Causal genes
EBF3
Part of
Hereditary diseaseMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
Also known as
developmental delay-ataxia-hypotonia-facial dysmorphism syndrome · EBF3 neurodevelopmental disorder · HADDS · hypotonia, ataxia, and delayed development syndrome; HADDS

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